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Brand Name :
Galopran, Alprida, Levusid, Mosar, Moza, M-pride, Omesap, Cilamos, Mic, Mosakind, Mosadrin, Mosamura
Synonyms :
mosapride
Class :
Gastrointestinal Agent, Prokinetic
Dosage Forms & StrengthsÂ
TabletÂ
2.5mgÂ
5mgÂ
No data is availableÂ
Dosage Forms & StrengthsÂ
TabletÂ
2.5mgÂ
5mgÂ
may have an increased risk of CNS depression when combined with almotriptan
may have an increased risk of CNS depression when combined with alprazolam
Actions and SpectrumÂ
Actions:Â
Spectrum:Â
mosapride is mainly indicated for the treatment of various gastrointestinal disorders, including:Â
Frequency not definedÂ
DiarrheaÂ
NauseaÂ
InsomniaÂ
ConstipationÂ
DizzinessÂ
Black Box Warning:Â
NoneÂ
Contraindication/Caution:Â
Contraindication:Â
Caution:Â
Pregnancy consideration:Â Â
Pregnancy Category: BÂ
Breastfeeding warnings:Â Â
It is unknown whether the drug is excreted in breast milk.Â
Pregnancy category:Â
Category A: Well-controlled and satisfactory studies show no risk to the fetus in the initial or later trimester.Â
Category B: There was no evidence of risk to the fetus in animal studies, and there were not enough studies on pregnant women.Â
Category C: There was evidence of risk of adverse effects in animal reproduction studies, and no adequate evidence in human studies must take care of potential risks in pregnant women.   Â
Category D: adequate data with sufficient evidence of human fetal risk from various platforms, but despite the potential risk, and used only in emergency cases for potential benefits.   Â
Category X: Drugs listed in this category outweigh the risks over benefits. Hence, these categories of drugs need to be avoided by pregnant women.   Â
Category N: No data is available for the drug under this category.Â
Pharmacology:Â Â
Pharmacodynamics:Â
Enhanced Gastric Emptying:Â
mosapride’s prokinetic action accelerates gastric emptying, which can be beneficial when delayed gastric emptying is a problem, such as gastroparesis.Â
Increased Peristalsis:Â
By stimulating peristalsis, mosapride aids in the rhythmic contractions of the small intestine, which helps propel food and digestive contents through the GI tract.Â
Lower Esophageal Sphincter (LES) Relaxation:Â
mosapride can relax the lower esophageal sphincter (LES), the muscular ring that separates the esophagus from the stomach. This action may help reduce symptoms of gastroesophageal reflux disease (GERD) by preventing the reflux of stomach contents into the esophagus.Â
Anti-emetic Action:Â
mosapride also has anti-emetic properties, meaning it can reduce nausea and vomiting, which is beneficial in conditions like functional dyspepsia and chemotherapy-induced nausea and vomiting.Â
Pharmacokinetics:Â
AbsorptionÂ
mosapride is well-absorbed after oral administration.Â
DistributionÂ
It is distributed widely in the body tissues, including the respiratory tract, soft tissues, and the skin.Â
MetabolismÂ
mosapride undergoes extensive first-pass metabolism in the liver. It is metabolized by various liver enzymes, including cytochrome P450 (CYP) enzymes, particularly CYP2D6.Â
Elimination and ExcretionÂ
The elimination half-life of mosapride is relatively short, typically ranging from 1.5 to 2.5 hours. This means that the drug is cleared from the body relatively quickly.Â
Administration:Â
mosapride is typically administered orally in tablets or capsules before meals to enhance gastrointestinal motility. It treats conditions like gastroparesis, functional dyspepsia, and GERD. Always follow the dosing instructions provided by your healthcare provider and consult them for any questions or concerns about its use.Â
Patient information leafletÂ
Generic Name: mosaprideÂ
Pronounced as: mo-zah-prydÂ
Why do we use mosapride?Â